Structure of PDB 1gsa Chain A Binding Site BS02
Receptor Information
>1gsa Chain A (length=314) Species:
37762
(Escherichia coli B) [
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MIKLGIVMDPIANINIKKDSSFAMLLEAQRRGYELHYMEMGDLYLINGEA
RAHTRTLNVKQNYEEWFSFVGEQDLPLADLDVILMRKDPPFDTEFIYATY
ILERAEEKGTLIVNKPQSLRDCNEKLFTAWFSDLTPETLVTRNKAQLKAF
WEKHSDIILKPLDGMGGASIFRVKEGDPNLGVIAETLTEHGTRYCMAQNY
LPAIKDGDKRVLVVDGEPVPYCLARIPQGGETRGNLAAGGRGEPRPLTES
DWKIARQIGPTLKEKGLIFVGLDIIGDRLTEINVTSPTCIREIEAEFPVS
ITGMLMDAIEARLQ
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1gsa Chain A Residue 320 [
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Receptor-Ligand Complex Structure
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PDB
1gsa
A pseudo-michaelis quaternary complex in the reverse reaction of a ligase: structure of Escherichia coli B glutathione synthetase complexed with ADP, glutathione, and sulfate at 2.0 A resolution.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
E281 N283
Binding residue
(residue number reindexed from 1)
E281 N283
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K125 K160 R210 R225 R233 D273 E281 N283
Catalytic site (residue number reindexed from 1)
K125 K160 R210 R225 R233 D273 E281 N283
Enzyme Commision number
6.3.2.3
: glutathione synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0004363
glutathione synthase activity
GO:0005524
ATP binding
GO:0016874
ligase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0006750
glutathione biosynthetic process
GO:0051289
protein homotetramerization
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1gsa
,
PDBe:1gsa
,
PDBj:1gsa
PDBsum
1gsa
PubMed
8810901
UniProt
P04425
|GSHB_ECOLI Glutathione synthetase (Gene Name=gshB)
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